Polymer-bound cobalt(II) porphyrins were studied for their dioxygen-binding
capacity. Tetra-aminoporphyrins were anchored on a divinylbenzene (DVB)-cr
osslinked chloromethyl polystyrene network. The crosslinked, solid polymers
were swelled in chloroform and the swollen polymers were used for the enti
re studies. Ortho-, meta- and para-substituted porphyrin systems were devel
oped by adjusting the bonding position with the help of suitably substitute
d aminoporphyrins. The products were characterized by chemical and spectros
copic methods. Cobalt(II) complexes of polymeric porphyrins were synthesize
d and characterized by electronic and ESR spectral methods. The spectra gav
e evidence for the systematic variation of electronic properties in ortho,
meta and para compounds and for the dioxygen-binding capacity of cobalt com
plexes. These results are discussed. Copyright (C) 1999 John Wiley & Sons,
Ltd.